ChemicalBook--->CAS DataBase List--->26272-83-3

26272-83-3

26272-83-3 Structure

26272-83-3 Structure
IdentificationBack Directory
[Name]

TOLUENE-4-SULFONIC ACID OXETAN-3-YL ESTER
[CAS]

26272-83-3
[Synonyms]

26272-83-3
3-Ts-oxetan
3-Oxetanyl tosylate
3-(tosyloxy)oxetane
3-Oxetanylp-toluenesulfonate,96%
3-Oxetanyl p-toluenesulfonate, 96%
3-Oxetanyl p-Toluenesulfonate
oxetan-3-yl 4-Methylbenzene-1-sulfonate
p-Toluenesulfonic Acid 3-Oxetanyl Ester
Oxetan-3-yl 4-methylbenzenesulfonate 98%
3-Oxetanol, 3-(4-methylbenzenesulfonate)
TOLUENE-4-SULFONIC ACID OXETAN-3-YL ESTER
4-methylbenzenesulfonic acid 3-oxetanyl ester
[Molecular Formula]

C10H12O4S
[MDL Number]

MFCD08544401
[MOL File]

26272-83-3.mol
[Molecular Weight]

228.265
Chemical PropertiesBack Directory
[Melting point ]

81.0 to 86.0 °C
[Boiling point ]

372℃
[density ]

1.34
[Fp ]

179°(354°F)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

White to Orange to Green
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

29309090
Spectrum DetailBack Directory
[Spectrum Detail]

TOLUENE-4-SULFONIC ACID OXETAN-3-YL ESTER(26272-83-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Oxetan-3-ol

7748-36-9

Tosyl chloride

98-59-9

TOLUENE-4-SULFONIC ACID OXETAN-3-YL ESTER

26272-83-3

General procedure for the synthesis of toluene-4-sulfonic acid oxetan-3-yl ester (14) from oxetan-3-ol (13) and p-toluenesulfonyl chloride: Step 1: To a 27 mL solution of dichloromethane containing 1.00 g (13.5 mmol) of oxetan-3-ol (13) and 7.6 mL (54.0 mmol) of triethylamine, 5.15 g (27.0 mmol) of p-toluenesulfonyl chloride was added. The reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, the reaction was quenched with 150 mL of saturated aqueous sodium bicarbonate and extracted with three 50 mL portions of dichloromethane. The organic phases were combined, concentrated and purified by column chromatography (silica, 0-25% ethyl acetate/hexane) to afford 1.22 g (94% yield) of toluene-4-sulfonic acid oxetan-3-yl ester (14) as a white solid. Its NMR hydrogen spectrum (CDCl3, 500 MHz) data were as follows: δ 7.78 (d, J=8.5 Hz, 2H), 7.36 (d, J=9.0 Hz, 2H), 5.29 (m, 1H), 4.69 (m, 4H), 2.46 (s, 3H).

[References]

[1] Patent: WO2012/138678, 2012, A1. Location in patent: Page/Page column 33
[2] Journal of Organic Chemistry, 1983, vol. 48, # 18, p. 2953 - 2956
[3] Patent: US2015/336982, 2015, A1. Location in patent: Paragraph 0290; 0291
[4] Patent: EP3342765, 2018, A1. Location in patent: Paragraph 0293
[5] Patent: US2008/9465, 2008, A1. Location in patent: Page/Page column 82
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